Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 12
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 9
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 9
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 7
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 6
rs3117582
BAG6 ; APOM
0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 6
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 6
rs2894207
LINC02571 ; HLA-B
0.882 0.160 6 31295974 intron variant T/C snv 0.20 6
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 5
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 5
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52 5
rs8034191
HYKK
0.695 0.440 15 78513681 intron variant T/C snv 0.27 5
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 4
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 4
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 4
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 4
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 4
rs735665
GRAMD1B
0.776 0.280 11 123490689 intron variant G/A snv 0.15 4
rs7501939
HNF1B
0.776 0.280 17 37741165 intron variant C/T snv 0.41 4
rs995030
KITLG
0.776 0.320 12 88496894 3 prime UTR variant A/G snv 0.67 4
rs1393350
LOC107984363 ; TYR
0.851 0.160 11 89277878 intron variant G/A snv 0.17 4
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 4
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 4
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 4